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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946Generated: October 26, 2026

Triethylamine → Methanesulfonic Acid

https://huagongshe.com/reaction/1946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-[Bis(5-cyclohexyl-4-hydroxy-2-methylphenyl)methyl]benzene-1,2-diolHCID 15789229—
Solvent1,4-DioxaneHCID 31275—
ProductMethanesulfonic AcidHCID 6395—
Product4-[Bis(5-cyclohexyl-4-hydroxy-2-methylphenyl)methyl]benzene-1,2-diolHCID 15789229—

Reaction Steps

Bis(5 -cyclohexyl-4-hydroxy-2-methylphenyl)-3,4-dihydroxyphenylmethane(1.0 mole), naphthoquinone-1,2-diazido-5-sulfonyl chloride (2.0 moles) and methanesulfonyl chloride(0.5 moles) were dissolved in dioxane (4,000 g). To the resulting solution, dioxane (1,500 g) having triethylamine (500 g) dissolved therein was added dropwise over 40 minutes at a controlled temperature not higher than 35° C. The precipitating salt was separated by filtration and the thus recovered reaction product was washed and dried to yield a mixed ester of bis(5-cyclohexyl-4-hydroxy-2-methylphenyl)-3,4-dihydroxyphenylmethane with naphthoquinone-1,2-diazido-5-sulfonic acid and methanesulfonic acid; the average degree of esterification was 50% for the quinonediazidosulfonate ester and 12% for the methanesulfonate ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728504
Source datasetuspto-grants-1998_03
ORD IDord-1a28675e5d044056be5059476c8f3ce9
Source noteuspto-grants-1998_03